Anis Khiat
Paris, France
Last Updated: 09/26/2026
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Found 8 publications
Loss of WNT2B Results in Epithelial Defects and Predisposes to Gastrointestinal Dysplasia in Humans.
Loss of WNT2B Results in Epithelial Defects and Predisposes to Gastrointestinal Dysplasia in Humans.
Journal: Cellular and molecular gastroenterology and hepatology
Published: July 23, 2024
Human ITGAV variants are associated with immune dysregulation, brain abnormalities, and colitis.
Journal: The Journal of experimental medicine
Published: March 25, 2024
Insights into the expanding intestinal phenotypic spectrum of SOCS1 haploinsufficiency and therapeutic options.
Journal: Journal of clinical immunology
Published: March 09, 2023
Generation of induced pluripotent stem cells (iPSCs) from a microvillus inclusion disease patient with a homozygous missense mutation in UNC45A.
Journal: Stem cell research
Published: August 03, 2022
Systemic inflammatory syndrome in children with FARSA deficiency.
Journal: Clinical genetics
Published: November 17, 2021
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking.
Journal: The Journal of clinical investigation
Published: September 15, 2021
Genetic Diagnosis Guides Treatment of Autoimmune Enteropathy.
Journal: Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
Published: August 27, 2021
Recent immunological literature under scrutiny by master students
Journal: Medecine sciences : M/S
Published: March 17, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026